Clinical Trials Directory

Trials / Completed

CompletedNCT04665232

Immunomodulatory Effects of Subcutaneous Progesterone in Patients Affected by Autoimmune Diseases

Immunomodulatory Effects of Subcutaneous Progesterone in Patients Undergoing IVF Affected by Autoimmune Diseases

Status
Completed
Phase
Study type
Observational
Enrollment
18 (actual)
Sponsor
San Carlo Public Hospital, Potenza, Italy · Academic / Other
Sex
Female
Age
18 Years – 42 Years
Healthy volunteers
Not accepted

Summary

This study evaluates the immunomodulatory effects of subcutaneous progesterone in patients undergoing IVF by determination of anti-nuclear antibodies (ANA),extractable nuclear antigen antibodies (ENA),anti- neutrophil cytoplasmic antibodies(ANCA),anti-DNA antibodies, anti-cardiolipin antibodies (ACA),Lupus anticoagulant antibodies (LAC) and C3 and C4 fractions of complement on the day of beta hCG dosage and during the eigth week of gestation.

Detailed description

The aqueous progesterone preparation for s.c. injection is the first systemic progesterone of its kind for the provision of luteal phase support (LPS) in patients undergoing IVF. The the high solubility and rapid absorption of the new preparation are enhanced using cyclodextrins that are starch residues with no therapeutic activity and with a particular molecular structure that closely resembles a 'cap'. Once absorbed after injection, the progesterone molecule is immediately dissociated from its cyclodextrin 'cap', remaining free in the circulation as if produced endogenously by the ovaries. In comparison to progesterone-in-oil preparation, the new aqueous solution administered by s.c.route resulted in a 3 fold higher and more rapid progesterone peak serum concentrations. The immunomodulating effects of progesterone are mediated outside of the pelvic cavity, on the peripheral cell of the immune system. For this reason only the injection procedure has this advantage Furthermore, the faster absorption rate and the higher peak serum concentration should increas the systemic immunomodulatory effect of subcutaneous progesterone compared to the vaginal and intramuscular administration

Conditions

Interventions

TypeNameDescription
DRUGaqueous subcutaneous progesterone25 mg/die of aqueous subcutaneous progesterone from the day of oocytes retrieval for two weeks.

Timeline

Start date
2014-04-01
Primary completion
2017-04-01
Completion
2017-04-01
First posted
2020-12-11
Last updated
2024-05-28

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT04665232. Inclusion in this directory is not an endorsement.